Assess the Knowledge of ALSVITAL-ENFNCT07207616
Level and Determinants of Advanced Life Support Knowledge Among Nurses
A study testing educational intervention for nursing in people with Assess the Knowledge of ALS, run by Universitat Jaume I at 1 site in Spain.
Trial summary
This study evaluated the knowledge of advanced life support (ALS) among general nurses in Spain and examined the effectiveness of an educational intervention to address identified knowledge gaps. Read more about this study
- Who is it for?
- Ages 22 to 65 years
- Conditions the study is for
- Assess the Knowledge of ALS
- What is being tested?
- educational intervention for nursing
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 38 participants
- Where
- 1 siteSpain
- Study dates
- 1 Nov 2020to 31 Oct 2023
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 22 to 65 years
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- active nursing professionals in the healthcare sector in the Valencian Community, including those working in care, management, teaching, and research roles.
- provide written informed consent before participating in the study.
Who cannot join
- Nurses who were not registered with an Official Nursing College in the Valencian Community
Trial locations and contacts
1 site in 1 country.
About this study
Official title: Level and Determinants of Advanced Life Support Knowledge Among Nurses in Spain and Effectiveness of an Educational Intervention for Nursing.
This study evaluated the knowledge of advanced life support (ALS) among general nurses in Spain and examined the effectiveness of an educational intervention to address identified knowledge gaps. Initially, a cross-sectional study was conducted between November 2020 and February 2021, involving 888 general nurses from all 52 Spanish provinces. Data were collected through a structured self-administered questionnaire assessing demographics, education, professional background, and theoretical ALS knowledge. The results showed that 72.3% of nurses did not achieve the minimum passing score of 70%, revealing significant knowledge deficits, particularly in fluid therapy, defibrillation protocols, ALS algorithms, and use of the LUCAS® CPR device. Higher knowledge levels were associated with female gender, possession of a Master's degree or higher, working in high-risk areas for cardiac arrest, and recent ALS training.
To address these gaps, a second, quasi-experimental study was carried out between February and October 2023 in the Valencian Community. This non-randomized intervention followed the TREND guidelines and targeted nurses registered in one of the three official nursing colleges of the region. The educational intervention included an asynchronous online phase hosted on a Google Sites platform, where participants accessed interactive learning materials and completed a pre-test. This was followed by a four-hour in-person session that included a brief theoretical review and hands-on workshops practicing various ALS techniques. A post-intervention test was administered immediately afterward. The intervention led to a noticeable improvement in ALS knowledge, demonstrating its effectiveness.
Overall, the study highlights insufficient ALS knowledge among Spanish nurses and the need for continuous, structured education. The successful outcome of the intervention reinforces the importance of ongoing training programs to enhance the preparedness of nurses in responding to cardiac arrest and other high-risk clinical scenarios.
Read the detailed description
Study design, area, and period A cross-sectional study was conducted from November 2020 to February 2021. The study population comprised nurses affiliated with all the official nursing associations in Spain, which are integrated at the national level in the General Council of the Official Nursing Associations of Spain (Consejo General de Colegios Oficiales de Enfermería de España). In this country, membership of one of these official nursing associations is compulsory for the practice of the profession. At the time of the study, the total number of registered nurses in Spain was 291,297.18 The actual sample size for the study was calculated using QuestionPro (https://www.questionpro.com/es/calculadorade-muestra.html#calculadora_de_muestra), considering a target population of 291,297 registered nurses in Spain, a confidence level of 95%, a margin of error of 5%, and an estimated missing rate of 15%. The calculated sample size was 443. A snowball sampling was applied. Data were collected consecutively for each nurse included, as all nurses willing to participate and meeting the study's inclusion criteria participated.
A structured self-administered questionnaire was used for data collection. This questionnaire contained three demographic questions, two questions related to professional experience, five questions regarding educational and ALS training background and professional experience, and 29 theoretical knowledge questions.
The set of 29 theoretical knowledge questions and their respective answer options are derived from a 30-item ERC test (see Supplemental material). This type of test is used in the training courses and assessment of nursing professionals to ensure an adequate level of knowledge of recommended best practice in emergency situations. Given the context, it was determined that a pretest of the instrument would not be conducted. Nevertheless, to avoid information bias, a validation of the content of our adapted and updated Spanish version of the test was conducted by a group of judges (n = 13) with experience in ALS.
For the second phase, a quasi-experimental study was designed between February and October 2023 in the Valencian Community. It was a non-randomized design with an educational intervention and pre-post intervention knowledge evaluation, following the TREND standard guidelines. The study population consisted of nurses registered with one of the three official nursing colleges in the Valencian Community, integrated at the regional level into the Nursing Council of the Valencian Community (CECOVA). At the time of the study, the total number of registered nurses in the Valencian Community was 21,265.
The study reached out to the Nursing Colleges of Castellón, Valencia, and Alicante via email to request their assistance in distributing the questionnaire among their members. Additionally, due to geographic availability, the Colleges of Castellón and Valencia were asked to provide their facilities for the educational intervention. The colleges agreed to distribute the questionnaire, sending the information to their members via email and through their official social media channels. Furthermore, the Castellón and Valencia colleges agreed to provide their facilities and materials for the educational intervention.
Due to challenges in recruiting participants for the in-person phase, contact was made with the Health Sciences Faculties of both the CEU Cardenal Herrera University of Castellón and Jaume I University of Castellón. Both institutions agreed to allow the use of their facilities and to disseminate the study among their employees.
The in-person educational intervention sessions took place at four different locations to facilitate participant attendance.
A non-probabilistic snowball sampling technique was used. The educational intervention was structured into two phases:
Online Phase: Using the Google Sites domain (https://sites.google.com/view/intervencion-sva/inicio), this phase was asynchronous, where participants accessed interactive educational materials and a pre-test on ALS. The online phase was designed to explain theoretical content, and a dedicated webpage was created for this purpose. Each enrolled participant was provided with a link to the site via email. Upon accessing the page, participants were guided on the steps they needed to follow to complete this phase properly.
In-person Phase: A 15-minute brief review of the theoretical content from the online phase was given at the start of this session. The session was then divided into different workshops where participants practiced various ALS techniques. At the end of the in-person session, participants completed a post-test questionnaire in the classroom. The duration of this phase was four hours.
Content of the Intervention:
Online Phase:
Pre-test questionnaire.
Reading theoretical content (CPR).
Solving interactive clinical cases.
Responding to the post-test (for those who did not attend the in-person phase). The estimated duration of this phase was about four hours. The pre- and post-tests were identical and consisted of 19 theoretical knowledge questions. These questions were derived from the 30-item ALS test, available in English (Appendix III). This type of test is used in training courses by the institution to ensure an adequate level of knowledge of best practices in emergency situations. For this study, the test was translated into Spanish and validated by 13 experts (judges) to prevent information bias. The profile of these judges and their recommendations are shown in Table 1. The interactive cases were created using the CANVA application. Furthermore, to ensure the validity of the test, the Cronbach's alpha coefficient for the instrument was determined, yielding a value of 0.670. The survey questionnaires were administered using Microsoft Forms, a survey management software, which was used to create and distribute the questionnaires.
In-person Phase: At the start of this phase, there was a brief 15-minute review of the theoretical content from the online phase. The session was then divided into various workshops where participants practiced different ALS techniques:
Intraosseous Access Workshop: Participants were introduced to the different materials and practiced the intraosseous access technique.
Arrhythmias Workshop: Using a CPR mannequin and a free arrhythmia simulator for PC (Arrhythmia Simulator), participants practiced integrated ALS scenarios.
Airway Management Workshop: Participants practiced endotracheal intubation techniques and familiarized themselves with different supraglottic devices as alternatives for intubation.
Final Scenario: Participants were divided into groups and tasked with integrating all previously learned content into a single clinical case that they had to resolve collectively.
Teaching Methods:
The first phase was conducted online, with the creation of a website using the Google Sites domain. The second phase took place in-person at the Official Nursing Colleges of Castellón and Valencia, as well as at CEU Cardenal Herrera University and Jaume I University.
- Conditions
- Assess the Knowledge of ALS
- Being tested
- educational intervention for nursing
- Keywords
- Advanced life support, Continuing education in nursing, Knowledge, Resuscitation
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
educational intervention for nursingOther
Also called Formative intervention
A quasi-experimental study was carried out between February and October 2023 in the Valencian Community. This non-randomized intervention followed the TREND guidelines and targeted nurses registered in one of the three official nursing colleges of the region. The educational intervention included an asynchronous online phase hosted on a Google Sites platform, where participants accessed interactive learning materials and completed a pre-test. This was followed by a four-hour in-person session that included a brief theoretical review and hands-on workshops practicing various ALS techniques. A post-intervention test was administered immediately afterward. The intervention led to a noticeable improvement in ALS knowledge, demonstrating its effectiveness.
| Study group | Role | What they receive |
|---|---|---|
| ON LINE | Experimental | Using the Google Sites domain (https://sites.google.com/view/intervencion-sva/inicio), this phase was asynchronous, where participants accessed interactive educational materials and a pre-test on ALS. The online phase was designed to explain theoretical content, and a dedicated webpage was created for this purpose. Each enrolled participant was provided with a link to the site via email. Upon accessing the page, participants were guided on the steps they needed to follow to complete this phase properly. Receives: Other: educational intervention for nursing |
| IN PERSON | Experimental | A 15-minute brief review of the theoretical content from the online phase was given at the start of this session. The session was then divided into different workshops where participants practiced various ALS techniques. At the end of the in-person session, participants completed a post-test questionnaire in the classroom. The duration of this phase was four hours. Receives: Other: educational intervention for nursing |
What is being measured
The primary outcome is the main question the study is designed to answer.
To determine the level of knowledge of nurses in Spain regarding Advanced Life Support (ALS) and identify the factors that influence it.
the study aims to assess the knowledge of ALS among general nurses in Spain and to identify the socio-educational and occupational factors influencing knowledge.
Measured: 6 hours
To assess the effectiveness of an educational intervention aimed at addressing the identified knowledge gaps in ALS.
the study aims to assess the effectiveness of an educational based in the identified gaps in ALS among general nurses in Spain.
Measured: 4 hours
Secondary outcomes (4)
To evaluate knowledge of ALS concepts and techniques.
the study aims to evaluate knowledge of ALS concepts based on ERC recommendations.
Measured: 30 minutes
To identify knowledge gaps in ALS.
the study aims to identify knowledge gaps in ALS according to the ERC recommendations.
Measured: 30 minutes
To determine the sociodemographic, occupational, and educational background characteristics that influence the level of knowledge about ALS.
the study aims To determine the sociodemographic, occupational, and educational background characteristics that influence the level of knowledge about ALS based on the ERC recommendations.
Measured: 30 minutes
To establish the effectiveness of using in-person clinical simulation as a complementary training strategy to online ALS education.
the study aims to establish the effectiveness of using in-person clinical simulation as a complementary training strategy to online ALS education based on ERC recommentations.
Measured: 4 hours
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted6 Oct 2025
- Study start1 Nov 2020
- Primary completion28 Feb 2021
- Study completion31 Oct 2023
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Assess the Knowledge of ALSStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Other
- Allocation
- Non-randomised
- Intervention model
- Parallel groups
- Masking
- Single blind
- Who is masked
- Participant
- Enrolment
- 38 participants (actual)
Sponsor and investigators
- Lead sponsor
- Universitat Jaume I
- Sponsor type
- University, hospital or other
- Collaborators
- Colegio oficial de Enfermeros y Enfermeras de Castellón, Cardenal Herrera University
- Responsible party
- Sponsor
- Investigators
- Paula Sanchez-Thevente, phD, Study director, Cardenal Herrera University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07207616
- Sponsor's protocol ID
- UCHCEU-UJI25
- Acronym
- VITAL-ENF
- Status last verified
- Oct 2026
- First submitted
- 14 Jul 2025
- Last updated
- 16 Oct 2026
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Yes: There is a first article published at SAGE OPEN MEDICINE: Level and determinants of advanced life support knowledge among nurses in Spain: A national cross-sectional study
Study at a glance
From the registry record, last updated by the sponsor on 16 Oct 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Level and Determinants of Advanced Life Support Knowledge Among Nurses in Spain and Effectiveness of an Educational Intervention for Nursing.
- ClinicalTrials.gov ID
- NCT07207616
- Acronym / sponsor ID
- VITAL-ENF / UCHCEU-UJI25
- Conditions
- Assess the Knowledge of ALS
- Keywords
- Advanced life support, Continuing education in nursing, Knowledge, Resuscitation
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 38 participants (actual)
- Lead sponsor
- Universitat Jaume IUniversity, hospital or other
- Collaborators
- Colegio oficial de Enfermeros y Enfermeras de Castellón, Cardenal Herrera University
- Study start
- 1 Nov 2020 (actual)
- Primary completion
- 28 Feb 2021 (actual)
- Study completion
- 31 Oct 2023 (actual)
- First posted
- 6 Oct 2025 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
This study evaluated the knowledge of advanced life support (ALS) among general nurses in Spain and examined the effectiveness of an educational intervention to address identified knowledge gaps. Initially, a cross-sectional study was conducted between November 2020 and February 2021, involving 888 general nurses from all 52 Spanish provinces. Data were collected through a structured self-administered questionnaire assessing demographics, education, professional background, and theoretical ALS knowledge. The results showed that 72.3% of nurses did not achieve the minimum passing score of 70%, revealing significant knowledge deficits, particularly in fluid therapy, defibrillation protocols, ALS algorithms, and use of the LUCAS® CPR device. Higher knowledge levels were associated with female gender, possession of a Master's degree or higher, working in high-risk areas for cardiac arrest, and recent ALS training.
To address these gaps, a second, quasi-experimental study was carried out between February and October 2023 in the Valencian Community. This non-randomized intervention followed the TREND guidelines and targeted nurses registered in one of the three official nursing colleges of the region. The educational intervention included an asynchronous online phase hosted on a Google Sites platform, where participants accessed interactive learning materials and completed a pre-test. This was followed by a four-hour in-person session that included a brief theoretical review and hands-on workshops practicing various ALS techniques. A post-intervention test was administered immediately afterward. The intervention led to a noticeable improvement in ALS knowledge, demonstrating its effectiveness.
Overall, the study highlights insufficient ALS knowledge among Spanish nurses and the need for continuous, structured education. The successful outcome of the intervention reinforces the importance of ongoing training programs to enhance the preparedness of nurses in responding to cardiac arrest and other high-risk clinical scenarios.
Detailed description
Study design, area, and period A cross-sectional study was conducted from November 2020 to February 2021. The study population comprised nurses affiliated with all the official nursing associations in Spain, which are integrated at the national level in the General Council of the Official Nursing Associations of Spain (Consejo General de Colegios Oficiales de Enfermería de España). In this country, membership of one of these official nursing associations is compulsory for the practice of the profession. At the time of the study, the total number of registered nurses in Spain was 291,297.18 The actual sample size for the study was calculated using QuestionPro (https://www.questionpro.com/es/calculadorade-muestra.html#calculadora_de_muestra), considering a target population of 291,297 registered nurses in Spain, a confidence level of 95%, a margin of error of 5%, and an estimated missing rate of 15%. The calculated sample size was 443. A snowball sampling was applied. Data were collected consecutively for each nurse included, as all nurses willing to participate and meeting the study's inclusion criteria participated.
A structured self-administered questionnaire was used for data collection. This questionnaire contained three demographic questions, two questions related to professional experience, five questions regarding educational and ALS training background and professional experience, and 29 theoretical knowledge questions.
The set of 29 theoretical knowledge questions and their respective answer options are derived from a 30-item ERC test (see Supplemental material). This type of test is used in the training courses and assessment of nursing professionals to ensure an adequate level of knowledge of recommended best practice in emergency situations. Given the context, it was determined that a pretest of the instrument would not be conducted. Nevertheless, to avoid information bias, a validation of the content of our adapted and updated Spanish version of the test was conducted by a group of judges (n = 13) with experience in ALS.
For the second phase, a quasi-experimental study was designed between February and October 2023 in the Valencian Community. It was a non-randomized design with an educational intervention and pre-post intervention knowledge evaluation, following the TREND standard guidelines. The study population consisted of nurses registered with one of the three official nursing colleges in the Valencian Community, integrated at the regional level into the Nursing Council of the Valencian Community (CECOVA). At the time of the study, the total number of registered nurses in the Valencian Community was 21,265.
The study reached out to the Nursing Colleges of Castellón, Valencia, and Alicante via email to request their assistance in distributing the questionnaire among their members. Additionally, due to geographic availability, the Colleges of Castellón and Valencia were asked to provide their facilities for the educational intervention. The colleges agreed to distribute the questionnaire, sending the information to their members via email and through their official social media channels. Furthermore, the Castellón and Valencia colleges agreed to provide their facilities and materials for the educational intervention.
Due to challenges in recruiting participants for the in-person phase, contact was made with the Health Sciences Faculties of both the CEU Cardenal Herrera University of Castellón and Jaume I University of Castellón. Both institutions agreed to allow the use of their facilities and to disseminate the study among their employees.
The in-person educational intervention sessions took place at four different locations to facilitate participant attendance.
A non-probabilistic snowball sampling technique was used. The educational intervention was structured into two phases:
Online Phase: Using the Google Sites domain (https://sites.google.com/view/intervencion-sva/inicio), this phase was asynchronous, where participants accessed interactive educational materials and a pre-test on ALS. The online phase was designed to explain theoretical content, and a dedicated webpage was created for this purpose. Each enrolled participant was provided with a link to the site via email. Upon accessing the page, participants were guided on the steps they needed to follow to complete this phase properly.
In-person Phase: A 15-minute brief review of the theoretical content from the online phase was given at the start of this session. The session was then divided into different workshops where participants practiced various ALS techniques. At the end of the in-person session, participants completed a post-test questionnaire in the classroom. The duration of this phase was four hours.
Content of the Intervention:
Online Phase:
Pre-test questionnaire.
Reading theoretical content (CPR).
Solving interactive clinical cases.
Responding to the post-test (for those who did not attend the in-person phase). The estimated duration of this phase was about four hours. The pre- and post-tests were identical and consisted of 19 theoretical knowledge questions. These questions were derived from the 30-item ALS test, available in English (Appendix III). This type of test is used in training courses by the institution to ensure an adequate level of knowledge of best practices in emergency situations. For this study, the test was translated into Spanish and validated by 13 experts (judges) to prevent information bias. The profile of these judges and their recommendations are shown in Table 1. The interactive cases were created using the CANVA application. Furthermore, to ensure the validity of the test, the Cronbach's alpha coefficient for the instrument was determined, yielding a value of 0.670. The survey questionnaires were administered using Microsoft Forms, a survey management software, which was used to create and distribute the questionnaires.
In-person Phase: At the start of this phase, there was a brief 15-minute review of the theoretical content from the online phase. The session was then divided into various workshops where participants practiced different ALS techniques:
Intraosseous Access Workshop: Participants were introduced to the different materials and practiced the intraosseous access technique.
Arrhythmias Workshop: Using a CPR mannequin and a free arrhythmia simulator for PC (Arrhythmia Simulator), participants practiced integrated ALS scenarios.
Airway Management Workshop: Participants practiced endotracheal intubation techniques and familiarized themselves with different supraglottic devices as alternatives for intubation.
Final Scenario: Participants were divided into groups and tasked with integrating all previously learned content into a single clinical case that they had to resolve collectively.
Teaching Methods:
The first phase was conducted online, with the creation of a website using the Google Sites domain. The second phase took place in-person at the Official Nursing Colleges of Castellón and Valencia, as well as at CEU Cardenal Herrera University and Jaume I University.
Study design
- Primary purpose
- Other
- Allocation
- Non-randomised
- Intervention model
- Parallel groups
- Masking
- Single blind (participant)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| ON LINE | Experimental | Other: educational intervention for nursingUsing the Google Sites domain (https://sites.google.com/view/intervencion-sva/inicio), this phase was asynchronous, where participants accessed interactive educational materials and a pre-test on ALS. The online phase was designed to explain theoretical content, and a dedicated webpage was created for this purpose. Each enrolled participant was provided with a link to the site via email. Upon accessing the page, participants were guided on the steps they needed to follow to complete this phase properly. |
| IN PERSON | Experimental | Other: educational intervention for nursingA 15-minute brief review of the theoretical content from the online phase was given at the start of this session. The session was then divided into different workshops where participants practiced various ALS techniques. At the end of the in-person session, participants completed a post-test questionnaire in the classroom. The duration of this phase was four hours. |
Who may qualify
- Ages
- 22 to 65 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (2 listed)
- active nursing professionals in the healthcare sector in the Valencian Community, including those working in care, management, teaching, and research roles.
- provide written informed consent before participating in the study.
Key exclusion criteria (1 listed)
- Nurses who were not registered with an Official Nursing College in the Valencian Community
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| educational intervention for nursingAlso: Formative interventionA quasi-experimental study was carried out between February and October 2023 in the Valencian Community. This non-randomized intervention followed the TREND guidelines and targeted nurses registered in one of the three official nursing colleges of the region. The educational intervention included an asynchronous online phase hosted on a Google Sites platform, where participants accessed interactive learning materials and completed a pre-test. This was followed by a four-hour in-person session that included a brief theoretical review and hands-on workshops practicing various ALS techniques. A post-intervention test was administered immediately afterward. The intervention led to a noticeable improvement in ALS knowledge, demonstrating its effectiveness. | Other | IN PERSON, ON LINE |
Primary outcome
To determine the level of knowledge of nurses in Spain regarding Advanced Life Support (ALS) and identify the factors that influence it.
Time frame: 6 hours
the study aims to assess the knowledge of ALS among general nurses in Spain and to identify the socio-educational and occupational factors influencing knowledge.
To assess the effectiveness of an educational intervention aimed at addressing the identified knowledge gaps in ALS.
Time frame: 4 hours
the study aims to assess the effectiveness of an educational based in the identified gaps in ALS among general nurses in Spain.
4 secondary outcomes
To evaluate knowledge of ALS concepts and techniques.
Time frame: 30 minutes
To identify knowledge gaps in ALS.
Time frame: 30 minutes
To determine the sociodemographic, occupational, and educational background characteristics that influence the level of knowledge about ALS.
Time frame: 30 minutes
To establish the effectiveness of using in-person clinical simulation as a complementary training strategy to online ALS education.
Time frame: 4 hours
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 16 Oct 2026.
- Individual participant dataSharing planned: Yes. There is a first article published at SAGE OPEN MEDICINE: Level and determinants of advanced life support knowledge among nurses in Spain: A national cross-sectional study
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Paula Sanchez-Thevente, phD study director
Cardenal Herrera University
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing educational intervention for nursing in people with Assess the Knowledge of ALS, run by Universitat Jaume I at 1 site in Spain.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 2 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 16 Oct 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Spain. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
To determine the level of knowledge of nurses in Spain regarding Advanced Life Support (ALS) and identify the factors that influence it. (time frame: 6 hours). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 16 Oct 2026.